25
Participants
Start Date
May 5, 2022
Primary Completion Date
August 1, 2024
Study Completion Date
August 1, 2024
CS1 Administration
CS1 delayed-release capsules will be supplied with 160 mg active pharmaceutical ingredient (sodium valproate) per capsule. Three dose levels that will be evaluated in this study; study drug will be administered as uneven, divided doses twice daily in the morning and in the evening (1/3 of the daily dose is to be administered between 7 and 9 am; 2/3 of the daily dose is to be administered between 7 and 9 pm).
Fredrik Frick, Gothenburg
Lead Sponsor
Collaborators (1)
Worldwide Clinical Trials
OTHER
Cereno Scientific AB
INDUSTRY